(19)
(11) EP 0 443 006 B1

(12) EUROPEAN PATENT SPECIFICATION

(45) Mention of the grant of the patent:
13.04.1994 Bulletin 1994/15

(21) Application number: 90913640.0

(22) Date of filing: 07.09.1990
(51) International Patent Classification (IPC)5A61K 7/16
(86) International application number:
PCT/US9005/083
(87) International publication number:
WO 9104/008 (04.04.1991 Gazette 1991/08)

(54)

ORAL RINSE AND METHOD FOR PLAQUE REMOVAL

MUNDWASSER UND VERFAHREN ZUR BESEITIGUNG DES ZAHNSTEINS

BAIN DE BOUCHE ET PROCEDE D'ELIMINATION DE LA PLAQUE


(84) Designated Contracting States:
AT BE CH DE DK ES FR GB IT LI LU NL SE

(30) Priority: 13.09.1989 US 406460

(43) Date of publication of application:
28.08.1991 Bulletin 1991/35

(73) Proprietor: CAMBRIDGE RESEARCH LABORATORIES, INC.
New York, NY 10022 (US)

(72) Inventors:
  • GERSHON, Sol
    Teaneck, NJ 07666 (US)
  • FOX, Charles
    Fairlawn, NJ 07410 (US)
  • GARFINKLE, Norton
    Boca Raton, FL 33432 (US)

(74) Representative: Onn, Thorsten et al
AB STOCKHOLMS PATENTBYRA Box 23101
104 35 Stockholm
104 35 Stockholm (SE)


(56) References cited: : 
EP-A- 0 137 436
US-A- 3 617 626
US-A- 4 532 124
US-A- 2 955 984
US-A- 4 097 604
US-A- 4 550 018
   
       
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description

    Background of the Invention



    [0001] This application relates to an oral rinse for the disruption of plaque from teeth, and relies upon applicants' discovery that the incorporation of orthophosphates leads to substantial removal of plaque.

    [0002] Dental plaque is present to a greater or lesser extent on virtually all dental surfaces. Dental plaque is composed of closely matted microorganisms in a matrix made from polysaccharides, proteins and other materials which are, at least in part, of salivary origin. The microorganisms are mainly coccoidal, especially in early plaque, changing in some mouths to filamentous organisms after a few days. Dental plaque presents a significant problem to dental health for several reasons. First, evidence indicates that the microorganisms in dental plaque are a primary factor in dental caries. In addition, the prime etiologic factor in periodontal disease, including gingivitis, is dental plaque.

    [0003] Moreover, dental plaque is a precursor in calculus formation. Dental calculus (tartar) forms on the surfaces of teeth at the gingival margin and promotes periodontal breakdown by increasing undesirable products in the crevicular pocket area. Supragingival calculus appears principally near orifices of salivary ducts e.g. on lingual surfaces of the lower anterior teeth, on buccal surfaces of the first and second molars, and on the distal surfaces of the posterior molars. In addition to being unsightly from an aesthetic viewpoint, calculus is a constant source of irritation to the gingiva and can make toothbrushing a painful procedure.

    [0004] Because of these problems associated with plaque, it is important to find means to reduce plaque accumulation on teeth. Regular brushing with a conventional dentifrice for some persons can retard or even prevent the accumulation of significant amounts of dental plaque and calculus. For other persons, however, the plaque film builds up rapidly even with regular brushing, which, in turn, leads to the formation of calculus. Removal by a dentist is the most common method available for individuals to prevent the undesirable consequences of the accumulation of significant amounts of dental calculus. Recently, however, dental rinses have been developed with the stated purpose of loosening plaque on dental surfaces to facilitate its removal during brushing. For example, U.S. Patent No. 4,657,758 describes a dental rinse which is an alkaline solution of a surfactant and a detergent builder.

    [0005] It has now been found that orthophosphates, particularly alkali metal orthophosphates and ammonium orthophosphates, when used in a concentration of about 1.2% to about 10.0% by weight in an oral rinse at pH 5.5 - 10.5, are highly effective in removing plaque on teeth. While orthophosphates have been used in dental preparations, the ability to act as plaque loosening and removing agents, to applicants' knowledge, has not been recognized. For example, alkali metal phosphate has been shown to be effective in reducing dental caries when added to cariogenic rodent diets. (Nizel et al., J. Dent Res. Supp. to No. 6, 43, 1123 (1964)). A similar result was noted in hamsters, along with the further observation that continuous administration of the phosphate supplement is required to attain this anticaries effectiveness (Englander et al., J. Dent. Res. 49(1), 140 (1970)). This effect has been attributed to a modification of the composition of the protein layer adsorbed on tooth enamel. (Pruitt et al., Nature 225, 1249 (1970)).

    [0006] Alkali metal phosphates have been used in fluoride dentifrices. U.S. Patent 4,198,394 claims a dentifrice containing sodium dihydrogen phosphate (0.03 - 0.4%) and stannous fluoride (0.03 - 0.4%) with a pH of about 2.5 to about 5.5. U.S. Patent 4,565,691 presents an oral hygiene composition which contains alkali metal phosphates in a fluoride-containing dentifrice which utilizes dicalcium phosphate dihydrate, as the abrasive. The phosphates are added to maintain fluoride availability. U.S. Patent 4,254,101 presents dentifrice formulas in which alkali metal phosphates are used as buffers in a fluoride-containing dentifrice. None of these patents are concerned with clear dental rinses or mouthwashes.

    [0007] Orthophosphates have also been used in certain oral rinses, to protect enamel. For example, an acidulated phosphate fluoride dental rinse from sodium fluoride, acidulated with a mixture of sodium phosphate, monobasic, and phosphoric acid to a level of 0.1M phosphate ion and a pH of 3.0 - 4.5 is recognized as an over-the-counter anticaries dental rinse drug product [Federal Register, 50 (No. 189):39854-39873, Sept. 30, 1985]. The phosphates are present to protect enamel at the low pH specified.

    Brief Description of the Invention



    [0008] The present invention provides an oral rinse intended for application to dental surfaces for the purpose of removing dental plaque, thereby retarding the accumulation of the plaque on dental surfaces. The oral rinse of this invention comprises an alkali metal orthophosphate or ammonium orthophosphate in an aqueous or aqueous-alcoholic solution with a pH of at least about 5.5 to about 10.5. Preferably, the oral rinse may also include an anionic surfactant in an amount from about 0.05% to about 3.0%, a nonionic surfactant in an amount at least about 0.05% to about 5.0% or both. The alkali metal orthophosphates or ammonium orthophosphates are present in an amount from 1.2% to about 10.0%. It has been found that when an alkali metal phosphate or ammonium phosphate is employed in the dental rinse or mouthwash described above, the ability of the formulation to remove plaque is surprisingly and significantly enhanced. The presence of an anionic or non-ionic surfactant facilitates penetration of the orthophosphates resulting in compositions providing significant removal of plaque from teeth.

    [0009] In further embodiments of the oral rinse of this invention, effective amounts of various conventional auxiliary materials such as colorants, flavorants, antiseptics and healing agents are advantageously employed in combination with other ingredients.

    [0010] The oral rinse of this invention may be applied to the surface of the teeth by any conventional process. Preferably, however, the oral rinse is applied by placing a comfortable amount of the oral rinse in the oral cavity and then circulating the rinse about the mouth with the intention of thoroughly soaking the teeth and gums. The substantial removal of oral plaque accomplished through the use of the dental rinse and associated methods of this invention should also serve to reduce the undesirable consequences associated with the buildup of dental plaque particularly gingivitis.

    [0011] Further advantages and objectives of this invention will be apparent from the detailed description of the invention which follows.

    Detailed Description of the Invention



    [0012] It has been discovered that compositions comprising the orthophosphates possess unexpected, significant abilities to remove dental plaque when used as an oral rinse. The term "oral rinse" as used herein encompasses both prebrushing dental rinses and mouthwashes which are generally used after brushing. The various components of such rinses are described below.

    Alkali Metal and Ammonium Phosphates



    [0013] The water-soluble phosphates useful in the current invention include monosodium orthophosphate, disodium orthophosphate, trisodium orthophosphate and the potassium and ammonium orthophosphate equivalents. A detailed description of these salts can be found in Kirk and Othmer, Encyclopedia of Chemical Technology, Third Edition, Volume 17, John Wiley and Sons (1982), pp. 426-472. The orthophosphate salts can exist in anhydrous or hydrated forms. Either form is acceptable for the desired compositions. The orthophosphate salts are used in the present compositions to provide at least 1.2% to about 10% by weight water soluble orthophosphate or mixtures thereof, preferably from about 1.5% to about 5%.

    Anionic Surfactants



    [0014] Organic surface-active agents are used in the compositions of the present invention to achieve increased prophylactic action and to assist in achieving thorough and complete dispersion of the orthophosphate salts throughout the oral cavity. Suitable examples of anionic surfactants are: water-soluble salts of higher fatty acid monoglyceride monosulfates, such as the sodium salt of the monosulfated monoglyceride of hydrogenated coconut oil fatty acids; higher alkyl sulfates such as sodium lauryl sulfate; alkyl aryl sulfonates; higher alkyl sulfoacetates; and higher fatty acid esters of 1,2 dihydroxypropane sulfonate. Ampholytic surfactants, serving as anions, can also be included in the compositions of the present invention. Examples of such compounds are: sodium or potassium N-lauroyl sarcosine; ethanolamine salts of N-lauroyl, N-myristoyl, or N-palmitoyl sarcosine. Mixtures of anionic surfactants can be employed.

    [0015] The anionic surfactants are used in the present compositions to provide at least about 0.05% to about 3% anionic compounds and preferably in the range from about 0.1% to about 1%. The preferred anionic surfactant, sodium lauryl sulfate, assists in achieving complete dispersion of the orthophosphate salts throughout the oral cavity and achieves an increase in plaque removal.

    Non-Ionic Surfactants



    [0016] Non-ionic surfactants are used in the compositions of the present invention to achieve prophylactic action, to assist in the dispersion of the orthophosphate salts throughout the oral cavity and to maintain removed plaque in a dispersed state to minimize redeposition on the teeth.

    [0017] Suitable examples of non-ionic surfactants are the Pluronics®, polyethylene oxide condensates of alkyl phenols, products derived from the condensation of ethylene oxide with the reaction product of propylene oxide and ethylene diamine, and ethylene oxide condensates of aliphatic alcohols. Also useful are mixtures of laurate esters of sorbitol and sorbitol anhydrides consisting predominantly of the monoester condensed with about 15-25 moles of ethyleneoxide. Tween® 20 available from I.C.I. Americas, Wilmington, Delaware is particularly useful. Mixtures of non-ionic surfactants can be employed with mixtures of anionic surfactants.

    [0018] The non-ionic surfactants are used in the present compositions to provide a concentration of at least about 0.05% to about 5% and preferably from about 0.1% to about 1%. The preferred non-ionic, polysorbate 20 (Tween® 20) assists in achieving dispersion of the orthophosphate salts throughout the oral cavity and maintains plaque in a dispersed state to minimize redeposition on the teeth.

    Auxiliary Materials



    [0019] Effective amounts of various conventional auxiliary materials such as colorants, flavorants, antiseptics and healing agents are advantageously employed in combination with other ingredients. More specifically, formulations of the oral rinse of this invention may include; (1) humectants, e.g. glycerin, sorbitol ; (2) sweetening agents, e.g. saccharin, aspartame, cyclamate; (3) flavors, e.g. oil of spearmint, oil of peppermint, menthol, methyl salicylate, oil of cinnamon; (4) coloring agents e.g. FD&C Blue No. 1; (5) detergent builders, e.g. sodium bicarbonate, sodium sulfate, ; (6) therapeutic agents, e.g. allantoin, soluble fluorides, urea, fluorophosphates, quaternary salts ; and (7) thickening agents, e.g. xanthan gum, sodium carboxymethylcellulose.

    [0020] The oral rinse is prepared by mixing the active ingredients together to form a homogeneous solution of the constituent ingredients. The rinse is used in a conventional manner, that is, by applying a comfortable amount in the mouth, say one tablespoonful, and rinsing it about the dental surfaces. As illustrated by the example below, a striking reduction in the amount of dental plaque on tooth surfaces is accomplished over a relatively brief usage period.

    [0021] The manner of making and using the present invention will be illustrated further by the following detailed example:



    [0022] The glycerin, saccharin sodium, sodium lauryl sulfate, disodium phosphate anhydrous, and monosodium phosphate monohydrate are intimately mixed until the solids are thoroughly wetted with the glycerin. The distilled water is added and the mixture stirred until clear and homogeneous. The flavor, polysorbate 20 and ethyl alcohol are mixed until clear and homogenous. The flavor mixture is added to the aqueous mixture with stirring during the addition. Stirring is continued until the mixture is clear and homogeneous. The resulting mixture is filtered.

    Example 2



    [0023] The following formulations were prepared for clinical evaluation to determine the effectiveness of each formula in removing plaque when 15 ml of product is used for 30 seconds.



    [0024] Formula A is the oral rinse presented in Example 1. Formula B is Formula A without the orthophosphate salts. A small quantity (0.25%) of sodium bicarbonate is used in Formula B to insure stability of the sodium lauryl sulfate. Sodium bicarbonate is not required in Formula A because the orthophosphates provide the desired sodium lauryl sulfate stability.

    [0025] Subjects were selected from a hospital outpatient dental clinic. All subjects were in good health, were between the ages of 18 and 60, and were able to follow instructions. Excluded were subjects who had oral lesions or systemically related gingival enlargement or who otherwise had oral conditions that interfere with an evaluation of the effects of the rinses. Scoring was done on teeth 3, 9, 12, 19, 25 and 28 (the Ramfjord teeth).

    [0026] On entry, each subject was scored for plaque on the Ramfjord teeth after application of a plaque disclosing solution. Plaque was scored by the Turesky modification of the Quigley-Hein plaque area index on the buccal and lingual surfaces. The subjects then rinsed for a timed 30 seconds with 15 ml of assigned rinse.

    [0027] After application of the plaque disclosing solution, a second plaque area assessment was made by the same scorer. The products supplied to the investigator were coded. Neither the investigator nor the subject knew the identity of the test product. Rinse A and rinse B were tested using randomly chosen subjects. Rinse A was evaluated with 105 subjects and rinse B was used by 50 subjects. The results are shown in Table I below.


       p = < .001 for A versus B

    [0028] The use of rinse B resulted in 5.3% removal of plaque, a small reduction effected by the presence of sodium lauryl sulfate and polysorbate 20. The use of rinse A according to the invention resulted in a 27.3% removal of plaque, a significant increase over rinse B. The improvement is due to the plaque removing effectiveness of the soluble orthophosphate salts. These studies demonstrate clearly that the addition of orthophosphates to the sodium lauryl sulfate and polysorbate 20 rinse results in a significantly greater removal of dental plaque, even in the absence of post rinse brushing.

    [0029] These data are also directly comparable with data published by L. Bailey, Clinical Preventive Dentistry 11(3):21-27(1989) in which Plax® a commercially available product in accordance with U.S. Patent 4,657,758 was compared with Listerine® antiseptic. These results were as follows:


    Thus, rinse A according to the invention is superior to the materials tested by Bailey.

    Example 3



    [0030] Another formulation was prepared as follows:



    [0031] Clinical testing of this formulation using the method of Example 2 with 104 subjects showed a 21.9% removal of plaque.

    [0032] The following examples further describe and demonstrate the embodiments within the scope of the present invention:

    Example 4



    [0033] 



    [0034] A similar formulation (Sodium Lauryl Sulfate 0.8%, polysorbate 20 1.5%, pH 7.45) showed some instability due to crystal growth on aging at room temperature.

    Example 5



    [0035] 




    Claims

    1. An oral rinse composition for removing plaque present on dental surfaces, characterized in that the composition contains from 1.2 % to 10 % by weight of alkali metal orthophosphate salts in an aqueous or an aqueous alcoholic carrier and has a pH of from about 5.5 to about 10.5.
     
    2. An oral rinse composition according to claim 1, characterized in that the amount of alkali metal orthophosphates is from 1.5 to 5 %.
     
    3. An oral rinse composition according to claims 1 to 2, characterized in that the alkali metal orthophosphates are selected from the group consisting of mono-, di-, and tri- sodium and potassium orthophosphates.
     
    4. An oral rinse composition according to claims 1-3, characterized in that the composition further comprises at least one surfactant selected from the group consisting of anionic and nonionic surfactants.
     
    5. An oral rinse composition according to claim 4, characterized in that the rinse comprises an anionic surfactant in an amount from about 0.05 % to about 3 %.
     
    6. An oral rinse composition according to claim 4 or 5, characterized in that the amount of anionic surfactant is from 0.1 % to 1 %.
     
    7. An oral rinse composition according to claims 4-6, characterized in that the anionic surfactant is sodium lauryl sulfate.
     
    8. An oral rinse composition according to claim 4, characterized in that the rinse comprises a nonionic surfactant in an amount from about 0.05 to about 5 % by weight.
     
    9. An oral rinse composition according to claim 8, characterized in that the nonionic surfactant is polyoxyethylene (20) - sorbitan mono laurate.
     
    10. An oral rinse composition according to claim 8 or 9, characterized in that the amount of nonionic surfactant is from about 0.1 % to about 1 %.
     
    11. An oral rinse composition according to claims 4, 5, 7, 8 and 9, characterized in that the rinse comprises form 0.05 to 3 % of an anionic surfactant and from 0.05 to 5 % of a nonionic surfactant.
     
    12. An oral rinse composition according to claims 1-11, characterized in that it further comprises one or more auxiliary, materials selected from the group consisting of sweetners, humectants, coloring agents, flavoring agents, detergent builders, therapeutic agents and thickening agents.
     
    13. An oral rinse composition according to claims 1-12, characterized in that it further comprises a water-soluble fluoride compound.
     
    14. An oral rinse composition according to claim 13, characterized in that the water-soluble fluoride compound is sodium fluoride.
     
    15. An oral rinse composition according to claim 13, characterized in that the water-soluble fluoride compound is sodium monofluorophosphate.
     
    16. An oral rinse composition for removing plaque present on dental surfaces characterized in that the composition comprises:

    (a) from 1.20 to 10 % by weight of ammonium orthophosphate salts; and

    (b) a surfactant selected from among anionic and non-ionic surfactants and combinations thereof 0.05 % to 8 % in an aqueous or an aqueous-alcoholic carrier for the ingredients of said dental rinse compositions, wherein the pH of said composition is about 5.5 to about 10.5.


     
    17. An oral rinse composition according to claim 16, characterized in that the orthophosphates are selected from the group consisting of mono-, di-, and tri-ammonium orthophosphates.
     
    18. An oral rinse composition for removing plaque present on dental surfaces characterized in that the composition comprises:

    (a) a plaque disrupting component consisting essentially of an alkali metal or ammonium ortrhophosphate or mixtures thereof in an amount of from 1.2 to 10 % by weight and from 0 to 8 % by weight of one or more surfactants selected from among anionic and nonionic surfactants; and

    (b) an aqueous or aqueous/alcoholic carrier.


     
    19. A composition according to claim 18, characterized in that it further comprises one or more auxiliary materials selected from among humectants, sweeteners, flavoring agents, coloring agents, detergent builders, therapeutic agents and thickening agents.
     
    20. A composition according to claims 18-19, characterized in that the plaque disrupting component includes from 0.05 to 3 % by weight of an anionic surfactant.
     
    21. A composition according to claims 18-20, characterized in that he plaque disrupting component includes from 0.05 to 5 % by weight of a nonionic surfactant.
     


    Ansprüche

    1. Mundspülung-Zusammensetzung zum Entfernen von auf Zahnoberflächen vorhandenem Belag,
    dadurch gekennzeichnet,
    daß die Zusammensetzung 1,2 bis 10 Gew.-% Alkalimetallorthophosphat-Salze in einem wässrigen oder einem wässrig-alkoholischen Träger enthält und einen pH von etwa 5,5 bis etwa 10,5 hat.
     
    2. Mundspülungs-Zusammensetzung nach Anspruch 1,
    dadurch gekennzeichnet,
    daß die Menge an Alkalimetallorthophosphaten 1,5 bis 5 % beträgt.
     
    3. Mundspülungs-Zusammensetzung nach den Ansprüchen 1 bis 2,
    dadurch gekennzeichnet,
    daß die Alkalimetallorthophosphate ausgewählt sind aus der Gruppe, die besteht aus Mono-, Di-, und Tri-Natrium- und Kaliumorthophosphaten.
     
    4. Mundspülungs-Zusammensetzung nach den Ansprüchen 1 bis 3,
    dadurch gekennzeichnet,
    daß die Zusammensetzung weiterhin mindestens ein oberflächenaktives Mittel aufweist, das ausgewählt ist aus der aus anionischen und nichtionischen oberflächenaktiven Mitteln bestehenden Gruppe.
     
    5. Mundspülungs-Zusammensetzung nach Anspruch 4,
    dadurch gekennzeichnet,
    daß die Spülung ein anionisches oberflächenaktives Mittel in einer Menge von etwa 0,05 % bis etwa 3 % aufweist.
     
    6. Mundspülungs-Zusammensetzung nach Anspruch 4 oder 5,
    dadurch gekennzeichnet,
    daß die Menge an anionischem oberflächenaktiven Mittel 0,1 % bis 1 % beträgt.
     
    7. Mundspülungs-Zusammensetzung nach den Ansprüchen 4 bis 6,
    dadurch gekennzeichnet,
    daß das anionische oberflächenaktive Mittel Natriumlaurylsulfat ist.
     
    8. Mundspülungs-Zusammensetzung nach Anspruch 4,
    dadurch gekennzeichnet,
    daß die Spülung ein nichtionisches oberflächenaktives Mittel in einer Menge von etwa 0,05 bis etwa 5 Gew.-% aufweist.
     
    9. Mundspülungs-Zusammensetzung nach Anspruch 8,
    dadurch gekennzeichnet,
    daß das nichtionische oberflächenaktive Mittel Polyoxyethylen (20) - sorbitanmonolaurat ist.
     
    10. Mundspülungs-Zusammensetzung nach Anspruch 8 oder 9,
    dadurch gekennzeichnet,
    daß die Menge an nichtionischem oberflächenaktiven Mittel etwa 0,1 % bis etwa 1 % beträgt.
     
    11. Mundpülungs-Zusammensetzung nach den Ansprüchen 4, 5, 7, 8 und 9,
    dadurch gekennzeichnet,
    daß die Spülung 0,05 bis 3 % eines anionischen oberflächenaktiven Mittels und 0,05 bis 5 % eines nichtionischen oberflächenaktiven Mittels aufweist.
     
    12. Mundspülungs-Zusammensetzung nach den Ansprüchen 1 bis 11,
    dadurch gekennzeichnet,
    daß sie weiterhin einen Hilfsstoff oder mehrere Hilfsstoffe aufweist, die ausgewählt sind aus der Gruppe, die besteht aus Süßungsstoffen, Anfeuchtemitteln, Farbstoffen, Geschmacksstoffen, Detergent-Buildern, therapeutischen Mitteln und Verdickungsmitteln.
     
    13. Mundspülungs-Zusammensetzung nach den Ansprüchen 1 bis 12,
    dadurch gekennzeichnet,
    daß sie weiterhin eine wasserlösliche Fluoridverbindung aufweist.
     
    14. Mundspülungs-Zusammensetzung nach Anspruch 13,
    dadurch gekennzeichnet,
    daß die wasserlösliche Fluoridverbindung Natriumfluorid ist.
     
    15. Mundspülungs-Zusammensetzung nach Anspruch 13,
    dadurch gekennzeichnet,
    daß die wasserlösliche Fluoridverbindung Natriummonofluorphosphat ist.
     
    16. Mundspülungs-Zusammensetzung zum Entfernen von auf Zahnoberflächen vorhandenem Belag,
    dadurch gekennzeichnet,
    daß die Zusammensetzung aufweist:

    (a) 1,20 bis 10 Gew.-% Ammoniumorthophosphat-Salze; und

    (b) 0,05 bis 8 % eines oberflächenaktiven Mittels, das ausgewählt ist unter anionischen und nichtionischen oberflächenaktiven Mitteln und Kombinationen davon, in einem wässrigen oder einem wässrig-alkoholischen Träger für die Bestandteile der Zahnspülungs-Zusammensetzung, wobei der pH der Zusammensetzung etwa 5,5 bis etwa 10,5 beträgt.


     
    17. Mundspülungs-Zusammensetzung nach Anspruch 16,
    dadurch gekennzeichnet,
    daß die Orthophosphate ausgewählt sind aus der Gruppe, die besteht aus Mono-, Di-, und Tri-Ammoniumorthophosphaten.
     
    18. Mundspülungs-Zusammensetzung zum Entfernen von auf Zahnoberflächen vorhandenem Belag,
    dadurch gekennzeichnet,
    daß die Zusammensetzung aufweist:

    (a) einen belagspaltenden Bestandteil, der im wesentlichen besteht aus einem Alkalimetall- oder Ammoniumorthophosphat oder Mischungen davon in einer Menge von 1,2 bis 10 Gew.-% und 0 bis 8 Gew.-% eines oberflächenaktiven Mittels oder mehrerer oberflächenaktiver Mittel, die ausgewählt sind unter anionischen und nichtionischen oberflächenaktiven Mitteln;

    (b) einen wässrigen oder wässrig-alkoholischen Träger.


     
    19. Zusammensetzung nach Anspruch 18,
    dadurch gekennzeichnet,
    daß sie weiterhin einen Hilfsstoff oder mehrere Hilfsstoffe aufweist, die ausgewählt sind unter Anfeuchtemitteln, Süßungsstoffen, Geschmacksstoffen, Farbstoffen, Detergent-Buildern, therapeutischen Mitteln und Verdickungsmitteln.
     
    20. Zusammensetzung nach den Ansprüchen 18 bis 19,
    dadurch gekennzeichnet,
    daß der belagspaltende Bestandteil 0,05 bis 3 Gew.-% eines anionischen oberflächenaktiven Mittels aufweist.
     
    21. Zusammensetzung nach den Ansprüchen 18 bis 20,
    dadurch gekennzeichnet,
    daß der belagspaltende Bestandteil 0,05 bis 5 Gew.-% eines nichtionischen oberflächenaktiven Mittels aufweist.
     


    Revendications

    1. Composition de bain de bouche destinée à l'élimination de la plaque présente sur les surfaces dentaires, caractérisée en ce que la composition contient 1,2 à 10 % en poids de sels orthophosphates de métaux alcalins dans un véhicule aqueux ou aqueux et alcoolique, et ayant un pH compris entre environ 5,5 et 10,5.
     
    2. Composition de bain de bouche selon la revendication 1, caractérisée en ce que la quantité d'orthophosphates de métaux alcalins est comprise entre 1,5 et 5 %.
     
    3. Composition de bain de bouche selon la revendication 1 ou 2, caractérisée en ce que les orthophosphates de métaux alcalins sont choisis dans le groupe qui comprend les orthophosphates monosodique, disodique, trisodique, monopotassique, dipotassique et tripotassique.
     
    4. Composition de bain de bouche selon l'une quelconque desrevendications 1 à 3, caractérisée en ce que la composition contient en outre au moins un agent tensioactif choisi dans le groupe qui comprend les agents tensioactifs anioniques et non ioniques.
     
    5. Composition de bain de bouche selon la revendication 4, caractérisée en ce que le bain de bouche contient un agent tensioactif anionique en quantité comprise entre environ 0,05 et 3 %.
     
    6. Composition de bain de bouche selon la revendication 4 ou 5, caractérisée en ce que la quantité de l'agent tensioactif anionique est comprise entre 0,1 et 1 %.
     
    7. Composition de bain de bouche selon l'une quelconque des revendications 4 à 6, caractérisée en ce que l'agent tensioactif anionique est le laurylsulfate de sodium.
     
    8. Composition de bain de bouche selon la revendication 4, caractérisée en ce que le bain de bouche contient un agent tensioactif non ionique en quantité comprise entre environ 0,05 et 5 % en poids.
     
    9. Composition de bain de bouche selon la revendication 8, caractérisée en ce que l'agent tensioactif non ionique est du polyoxyéthylène(20)-monolaurate de sorbitanne.
     
    10. Composition de bain de bouche selon la revendication 8 ou 9, caractérisée en ce que la quantité d'agent tensioactif non ionique est comprise entre environ 0,1 et 1 % environ.
     
    11. Composition de bain de bouche selon l'une quelconque des revendications 4, 5, 7, 8 et 9, caractérisée en ce que le bain de bouche contient 0,05 à 3 % d'un agent tensioactif anionique et 0,05 à 5 % d'un agent tensioactif non ionique.
     
    12. Composition de bain de bouche selon l'une quelconque des revendications 1 à 11, caractérisée en ce qu'il contient en outre une ou plusieurs matières auxiliaires choisies dans le groupe qui comprend des agents sucrants, humidifiants, colorants, aromatisants, les adjuvants pour détergents, les agents thérapeutiques et les agents épaississants.
     
    13. Composition de bain de bouche selon l'une quelconque des revendications 1 à 12, caractérisée en ce qu'elle contient en outre un composé de fluorure hydrosoluble.
     
    14. Composition de bain de bouche selon la revendication 13, caractérisée en ce que le composé hydrosoluble de fluorure est le fluorure de sodium.
     
    15. Composition de bain de bouche selon la revendication 13, caractérisée en ce que le composé hydrosoluble de fluorure est le monofluorophosphate de sodium.
     
    16. Composition de bain de bouche destinée à l'élimination de la plaque présente sur les surfaces des dents, caractérisée en ce que la composition comprend :

    (a) 1,20 à 10 en poids de sels orthophosphates d'ammonium, et

    (b) un agent tensioactif choisi parmi les agents tensioactifs anioniques et non ioniques et leurs combinaisons à raison de 0,05 à 8 % dans un véhicule aqueux ou aqueux et alcoolique en ce qui concerne les ingrédients des compositions de bain de bouche, le pH de la composition étant d'environ 5,5 à 10,5.


     
    17. Composition de bain de bouche selon la revendication 16, caractérisée en ce que les orthophosphates sont sélectionnés dans le groupe qui comprend les orthophosphates de mono, di et tri ammonium.
     
    18. Composition de bain de bouche destinée à l'élimination de la plaque présente sur les surfaces des dents, caractérisée en ce que la composition comprend :

    (a) un élément constituant de rupture de plaque constitué essentiellement d'un orthophosphate de métal alcalin ou d'ammonium ou de mélanges d'orthophosphates en quantité comprise entre 1,2 et 10 % en poids et 0 à 8 % en poids d'un ou plusieurs agents tensioactifs choisis parmi les agents tensioactifs anioniques et non ioniques, et

    (b) un véhicule aqueux ou aqueux et alcoolique.


     
    19. Composition selon la revendication 18, caractérisée en ce qu'elle contient en outre une ou plusieurs matières auxiliaires choisies parmi les agents humidifiants, sucrants, aromatisants, colorants, les adjuvants pour détergents, les agents thérapeutiques et les agents épaississants.
     
    20. Composition selon la revendication 18 ou 19, caractérisée en ce que l'élément constituant de rupture de la plaque contient 0,05 à 3 % en poids d'un agent tensioactif anionique.
     
    21. Composition selon l'une quelconque des revendications 18 à 20, caractérisée en ce que l'élément constituant de rupture de la plaque contient 0,05 à 5 % en poids d'un agent tensioactif non ionique.